feasibility study of sequential adjuvant chemotherapy … study of sequential adjuvant chemotherapy...
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Feasibility study of sequential adjuvant chemotherapy with three months oxaliplatin-based regimen (modified FOLFOX6 or CAPOX) followed by three months capecitabine in patients with stage III and high risk stage II colorectal cancer: (JSWOG C2)
Hiroaki Tanioka1), Kazuki Yamashita2), Akihito Tsuji3), Hideo Okumura4), Yasuo Oka4), Atsushi Tsuruta4), Michio Inukai5), Toshiki Yamakawa6), Tomoki Yamatsuji7), Yoshimitsu Masanori8), Kazuhiro Toyota9), Taketoshi Yamano10), Yuji Yamamoto11), Takeshi Nagasaka12), Masazumi Okajima13)
1) Department of Medical Oncology, Okayama Rosai Hospital, 2)Department of Surgery, Okayama Rosai Hospital ,3) Department of Medical Oncology, Kobe City Medical Center General Hospital ,4) Department of Digestive Surgery, Kawasaki Medical School Hospital , 5) Department of General Medicine, Kagawa University Hospital, 6) Department of Surgery, Kagawa Prefectural Central Hospital, 7) Department of General Surgery, Kawasaki Medical School, 8) Department of Surgery, Hiroshima City Asa Hospital , 9) Department of Surgery, National Hospital Organization Higashihirosima Medical Center , 10) Department of Surgery, Kurashiki Medical Center , 11) Department of Digestive Surgery Oncology, Ehime University Hospital, 12) Department of Digestive Surgery, Okayama University Hospital, 13) Department of Surgery, Hiroshima City Hospital
BackgroundSix months oxaliplatin (OX)-based chemotherapy
(modified FOLFOX6 or CAPOX) is the standard adjuvant chemotherapy for completely resected stage III colorectal cancer (CRC) in Japan.
However neurotoxicity is the most frequent toxicity of these chemotherapy regimens and often decline their QOL.
OX induced neurotoxicity is well known to be appeared by dose-dependently and progresses to irreversible in some cases.
Six months OX regimen has been reported to leave neurotoxicity after treatment in patients with cmpletely resected stage III CRC.
References:1) Daniel G. Haller. et al., J Clin Oncol. Apr 10, 2011:1465-14712) Nadine J. McCleary. et al., J Clin Oncol. Jul 10, 2013:2600-26063) Thierry Andre. Et al., N Engl J Med 350:2343 51,2004.4) Thierry Andre. et al., J Clin Oncol. Jul 1, 2009:3109-31165) Kuebler JP, et al., J Clin Oncol.2007; 256) J. Philip Kuebler. et al., J Clin Oncol. 2007 Jun 1;25(16):2205-117) Yothers G. et al., J Clin Oncol. 2011
ObjectivesTo investigate the feasibility of sequential
approach with three months OX-based regimen followed by three months capecitabine in Japanese patients with stage III CRC, in addition to high-risk stage II CRC. (UMIN000004934 )
Primary endpoint
・ Frequency and Grade of peripheral sensory and motor neuropathy (PSN/PMN) (CTCAE v4 and PNQ)
Secondary endpoints
・Proportion of completion in oxaliplatin base therapy
・Proportion of completion in adjuvant chemotherapy
・ Proportion of treatment selection
・ Adverse event
・ Compare FOLFOX to CAPOX in efficacy or adverse event
• Physician’s evaluation with CTCAE has a tendency toward down grading and Patient-reported outcomes are important for detecting adverse events.
• Patient Neurotoxicity Questionnaire (PNQ) to evaluate the neurotoxityof OX is a self-reported questionnaire.
Eligibility
Study Design
mFOLFOX6 6 cyclesOX 85mg/m2, L-LV 200mg/m2, Bolus 5FU 400mg/m2 on day 1
Infusional 5FU 2400mg/m2.on day 1-2, q2w
CAPOX 4 cyclesOX 130mg/m2 on day 1
Capecitabine 2000mg/m2 on day 1-14, q3w
Capecitabine 4 cycles2500 mg/m2 or continuous dose on day 1-14, q3w
PNQ 1.5M 3Mbaseline 6M
CTCAEEvery cycle
Main inclusion criteria
・histopathologically confirmed colorectal cancer.
・ StageIII (or high risk stageII) and R0 resection.
・ After resection, it is possible to begin the adjuvant chemotherapy within 8 weeks
・ Age: ≧20 years
・ ECOG PS: 0-1
Main exclusion criteria
・more than grade 1 (CTCAE v4.0) PN
Statistical Design
While attempting to detect a frequency of 3.9%
with 95% probability for the occurrence of PSN
(≧Grade 3 CTCAE), we determined that the
sample size would include 80 patients.
Results
Consort flow diagram Characteristics of the patients
Patients enrolled (n=91)
On treatment (n=86)
Eligible patients (n=86)
Not fulfill the eligibility (n=2)Reject treamtment (n=3)
91 patients enrolled in 11 institutes (between 2011 and 2014)All patinets (n=86)
Age median (range) 65 (36-81)
ECOG PS(0/1) 81/5
Sex (Male/Female) 49/37
Tumor site (rectal/non-rectal) 32/54
Histologic appearance(well/mod/por/others)
14/65/5/2
Disease stage (Ⅱ/Ⅲa/Ⅲb) 15/47/24
All patients mFOLFOX6 CAPOX P value
Number 86 30 56
Proportion of completion
(%)
OX-based therapy 83.7 80.0 85.7 0.544
All treatments 65.1 63.3 66.1 0.816
Median dose of OX(range) mg/m2
479(82-531)
467(82-512)
490(120-531)
0.123
%
All Patients mFOLFOX6(n=30) CAPOX(n=56)P value(Fisher test:
All grade)
All G3≦ All G3≦ All G3≦
HFS 50.0 3.5 63.3 3.3 42.9 3.6 0.113
Anorexia 47.7 4.7 56.7 0.0 42.9 7.1 0.262
Diarrhea 26.7 8.1 23.3 10.0 28.6 7.1 0.799
Nausea 30.2 1.2 26.7 0.0 32.1 1.8 0.632
MucositisOral
25.6 1.2 46.7 3.3 14.3 0.0 0.001
PSN 81.4 3.5 86.7 3.3 78.6 3.6 0.402
PMN 22.1 1.2 16.7 0.0 25.0 1.8 0.427
%
All Patients mFOLFOX6(n=30) CAPOX(n=56)P value(Fisher test:
All grade)
All G3≦ All G3≦ All G3≦
leukopenia 34.9 0.0 33.3 0.0 35.7 0.0 1.000
neutropenia 57.0 9.3 53.3 3.3 58.9 12.5 0.653
anemia 53.5 0.0 70.0 0.0 44.6 0.0 0.040
thrombocytopenia
62.8 2.3 60.0 3.3 64.3 1.8 0.816
T-bil 9.3 0.0 6.7 0.0 10.7 0.0 0.708
AST 67.4 0.0 73.3 0.0 64.3 0.0 0.473
ALT 47.7 5.8 56.7 6.7 42.9 5.4 0.262
ALP 25.6 1.2 16.7 0.0 30.4 1.8 0.202
Cre 8.1 1.2 13.3 3.3 5.4 0.0 0.232
Proportion of completion and Dose of OX
Adverse Events
Frequency of severity (PSN, PMN)
0
5
10
15
20
25
30
1.5M 3Mbaseline 6M
Pro
po
rtio
n(%)
Assessnment Point
PNQ-PSN
CTCAE-PSN
PNQ-PMNCTCAE-PMN
PNQ grade C≦CTCAE grade 2≦
Correlation between PNQ and CTCAE
PMN PNQ CTCAE
PNQ 1.0 -
CTCAE 0.127 1.0
PSN PNQ CTCAE
PNQ 1.0 -
CTCAE 0.468 1.0
The proportion of grade3 PSN (3.3%) and PMN (1.2%) during treatment was lower
than 6 months OX-based adjuvant treatment previously reported.
At 6 months after the end of treatment, there was no grade3 PSN patient.
Sequential approach with 3 months OX-based regimen followed by 3 months
capecitabine is a safety adjuvant treatment for CRC.
PNQ appears to detect OX induced neurotoxicity earlier than CTCAE.
conclusions
PSN during treatment and after 6 Mo follow-up
Spearman’s correlation cofficient
0
50
100Grade 3Grade 1+2
During Treatment6 Mo
Follow-up
3.5%
77.9% 0%
25.3%
Pro
po
rtio
n(%)
0
50
100
Acknowledgement This study was supported by Japan Southwest Oncology Research Support Organization (JSWOGORG). We would like to thank all participating patients and investigators participated in this study.
P-246
Study RegimenProportion of completion in therapy (%)
Median doseof OX
( mg/m2)
PSN during treatment
All grade (G3/4) (%)
XELOXA(NO16968)1) 2)
XELOX(n=942)
69874
(max1040)78
(11)
MOSAIC3)4)
FOLFOX4(n=1108)
74.7810
(max 1020)
92 (12.5)
18.1 (0.6)3yr
NSABPC-075)6)7)
FLOX(n=1247)
-677
(max 765)
85.3 (8.4)
29.9 (0.4)1yr
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